718-71-8 Usage
Description
Ethylphenylcyano-acetic acid ethyl ester, also known as Ethyl Cyanoethylphenylacetate (CAS# 718-71-8), is a chemical compound that is characterized by its yellowish oil appearance. It is primarily used in the field of organic synthesis, where it serves as a valuable intermediate for the creation of various other compounds.
Uses
Used in Organic Synthesis:
Ethylphenylcyano-acetic acid ethyl ester is used as a synthetic intermediate for the production of various organic compounds. Its unique chemical structure allows it to be a versatile building block in the synthesis of a wide range of molecules, making it an essential component in the chemical industry.
Used in Pharmaceutical Industry:
Ethylphenylcyano-acetic acid ethyl ester is used as a key component in the development of new pharmaceuticals. Its ability to be modified and incorporated into various drug molecules makes it a valuable asset in the design and synthesis of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, Ethylphenylcyano-acetic acid ethyl ester is utilized as a starting material for the synthesis of various agrochemicals, such as pesticides and herbicides. Its role in this industry is crucial for the development of new and effective products to protect crops and enhance agricultural productivity.
Used in Dye and Pigment Industry:
Ethylphenylcyano-acetic acid ethyl ester is also employed in the dye and pigment industry as a precursor for the synthesis of various dyes and pigments. Its unique chemical properties make it suitable for the production of a wide range of colors and shades, contributing to the diversity of products available in this market.
Check Digit Verification of cas no
The CAS Registry Mumber 718-71-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 718-71:
(5*7)+(4*1)+(3*8)+(2*7)+(1*1)=78
78 % 10 = 8
So 718-71-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NO2/c1-3-13(10-14,12(15)16-4-2)11-8-6-5-7-9-11/h5-9H,3-4H2,1-2H3
718-71-8Relevant articles and documents
Tert-Butoxide-Mediated Arylation of 2-Substituted Cyanoacetates with Diaryliodonium Salts
Qian, Xiaofei,Han, Jianwei,Wang, Limin
, p. 940 - 946 (2016/04/05)
A transition metal-free direct arylation of 2-substituted cyanoacetates with diaryliodonium salts was developed. With this approach, a wide range of α-tolunitrile derivatives has been synthesized in good to excellent yields of 45-92%. Furthermore, the practicability of this approach is further manifested in the synthesis of a related bioactive agent of glutarimide.
Nucleophile generation via decarboxylation: Asymmetric construction of contiguous trisubstituted and quaternary stereocenters through a Cu(I)-catalyzed decarboxylative mannich-type reaction
Yin, Liang,Kanai, Motomu,Shibasaki, Masakatsu
supporting information; experimental part, p. 9610 - 9611 (2011/03/19)
(Chemical Equation Presented) The first catalytic asymmetric decarboxylative Mannich-type reaction between aldimines and cyanocarboxylic acids was developed. α,α,β-Trisubstituted β-amino nitriles containing contiguous trisubstituted and all-carbon quatern
Selective Mono-methylation of Arylacetonitriles and Methyl Arylacetates by Dimethyl Carbonate
Selva, Maurizio,Marques, Carlos Alberto,Tundo, Pietro
, p. 1323 - 1328 (2007/10/02)
Both arylacetonitriles and methyl arylacetates react with dimethyl carbonate (DMC) (20 molar excess) at 180 - 200 deg C in the presence of K2CO3 to produce monomethylated 2-arylpropionitriles and methyl 2-arylpropionates, respectively, with a selectivity >99.5percent.The reaction, with wide application, proceeds by DMC acting as a methoxycarbonylating agent towards the ArCH-X anion (X = CN, CO2Me) and as a methylating agent to ArC-(CO2Me)X.DMC also proved to be the best solvent for such reactions.
